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SM16, an orally active TGF-beta type I receptor inhibitor prevents myofibroblast induction and vascular fibrosis in the rat carotid injury model.

   
Author Kai Fu,Michael J Corbley,Lihong Sun,Jessica E Friedman,Feng Shan,James L Papadatos,Donald Costa,Frank Lutterodt,Harry Sweigard,Scott Bowes,Michael Choi,P Ann Boriack-Sjodin,Robert M Arduini,Dongyu Sun,Miki N Newman,Xiamei Zhang,Jonathan N Mead,Claudio E Chuaqui,H-Kam Cheung,Xin Zhang,Mark Cornebise,Mary Beth Carter,Serene Josiah,Juswinder Singh,Wen-Cherng Lee,Alan Gill,Leona E Ling
Citation Information Arteriosclerosis, thrombosis, and vascular biology, 28: (2008)
Keywords Activin Receptors, Type I,Adenosine Triphosphate,Administration, Oral,Animals,Azabicyclo Compounds,Binding Sites,Carotid Artery Injuries,Cell Line,Fibroblasts,Fibrosis,Humans,Male,Myoblasts, Smooth Muscle,Protein Kinase Inhibitors,Protein-Serine-Threonine Kinases,Rats,Rats, Sprague-Dawley,Receptors, Transforming Growth Factor beta,Transforming Growth Factor beta
Related Products 30-011
Pub Med ID 18202322
   

Abstract

TGF-beta plays a significant role in vascular injury-induced stenosis. This study evaluates the efficacy of a novel, small molecule inhibitor of ALK5/ALK4 kinase, in the rat carotid injury model of vascular fibrosis.